US20040143038A1 - Age-stable composition having a polysaccharide - Google Patents

Age-stable composition having a polysaccharide Download PDF

Info

Publication number
US20040143038A1
US20040143038A1 US10/346,267 US34626703A US2004143038A1 US 20040143038 A1 US20040143038 A1 US 20040143038A1 US 34626703 A US34626703 A US 34626703A US 2004143038 A1 US2004143038 A1 US 2004143038A1
Authority
US
United States
Prior art keywords
percent
composition
weight
polysaccharide
binder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/346,267
Other languages
English (en)
Inventor
Thomas Aberle
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
National Starch and Chemical Investment Holding Corp
Original Assignee
National Starch and Chemical Investment Holding Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by National Starch and Chemical Investment Holding Corp filed Critical National Starch and Chemical Investment Holding Corp
Priority to US10/346,267 priority Critical patent/US20040143038A1/en
Assigned to NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION reassignment NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ABERLE, THOMAS
Priority to PCT/US2004/000461 priority patent/WO2004065320A2/fr
Priority to EP04700899A priority patent/EP1583725A2/fr
Publication of US20040143038A1 publication Critical patent/US20040143038A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24Macromolecular compounds
    • C04B24/38Polysaccharides or derivatives thereof

Definitions

  • This invention relates to a composition having a polysaccharide, an organic polymer binder, and an aging stabilizer.
  • the aging-stabilizer allows the composition to maintain a nearly constant initial wetted viscosity, independent of the storage time of the dry composition.
  • the composition is preferably a gypsum plaster or a gypsum-free and cement-free plaster containing a film-forming polymer.
  • compositions such as plasters, and mortars, generally contain a binder and filler.
  • the composition often includes a number of additives that improve the working and finished properties of the composition.
  • U.S. Pat. No. 6,409,825 describes several wet gypsum accelerators, including glycine, and sodium D-gluconate.
  • U.S. Pat. No. 6,080,806 describes the addition of redispersible carboxylic-functional polymers and amino acids to mortar or concrete.
  • the dried polymer/amino acid mixture is stable on storage without agglomeration.
  • polysaccharides There is no mention of polysaccharides in the formulations or any issues of storage stability.
  • U.S. Pat. No. 6,402,832 describes a gypsum wallboard joint compound containing water soluble cationic polymers having nitrogen (amine or substituted amine) groups to reduce the moisture content and improve the strength of finished wallboard.
  • Polysaccharides are often used as plaster additives to improve water retention, consistency, adhesion and plasticization. Even small amounts of polysaccharides can delay the rapid uptake of water by the adsorbent substrate, ensuring that the water remains present for uniform setting and hardening. This prevents the premature drying of the plaster, permitting longer working times.
  • U.S. Pat. No. 5,932,001 describes a plaster containing an amylaceous additive that is effective as a plaster thickener. There is no recognition of an initial viscosity loss related to dry storage time, and no mention of a compound providing aging stability.
  • composition comprising from 0.01 to 99.9 percent by weight of at least one polysaccharide; 0.0001 to 50 percent by weight, of at least one aging stabilizer; and from 0.1 to 99.9 percent by weight of at least one organic polymer binder, all weight percentages based on the amount of dry composition solids.
  • the invention also relates to a method for increasing the age stability of a dry building composition containing at least one polysaccharide, by combining into said dry composition an aging stabilizer.
  • compositions of the present invention are pliable mixtures of various materials with water, which dry or set to form a coherent solid.
  • the composition may be used as building compositions in the form of a plaster or mortar, generally containing gypsum, lime, or a film-forming polymer.
  • aging stability and “age-stable” as used herein is meant that the initial viscosity of a wetted dry powder composition remains nearly constant, regardless of the length of time the dry composition is stored or “aged”.
  • An age stable composition can be defined as one which when stored as a dry mix in a sealed container at 40° C. for 10 days and mixed with water will have an initial viscosity that is reduced by no more than 25 percent of the viscosity of an un-aged mixture, and preferably by no more than 15 percent of the un-aged mixture.
  • “aging stability” and “age-stability” as used herein is meant that the paste retains essentially the same viscosity for at least six months. Essentially the same viscosity meaning less than a 15 percent decrease in viscosity of the paste over a six month period when stored in a sealed container at standard conditions of 23° C. and 50 percent relative humidity.
  • aging stabilizer is meant a compound or compounds added to a composition containing a polysaccharide and a binder, which causes the composition to have age stability as defined above.
  • the aging stabilizer does not encompass biocides.
  • the invention relates to a composition containing polysaccharide, binder, and aging stabilizer.
  • the invention preferably relates to an age-stable dry plaster or mortar, gypsum or gypsum-free composition.
  • Polysaccharides are used in building compositions to improve water retention, consistency, adhesion and plasticization.
  • Polysaccharides useful in the composition of the invention include starches and modified starches, cellulose, cellulose ethers, xanthan gum, guar gum, guar ethers, alginates, and Wellan gums. Particularly useful polysaccharides are cellulose ethers and guar ethers.
  • Useful cellulose ethers include, but are not limited to methylcellulose (MC), ethyl cellulose (EC), hydroxyethyl cellulose (HEC), hydroxypropyl cellulose (HPC), methylhydroxyethylcellulose MH EC), ethyl hydroxyethyl cellulose (EH EC), ethylhydroxypropyl cellulose (EHPC), methylhydroxyethylcellulose MHEC), methylhydroxypropylcellulose (MHPC), and carboxymethyl cellulose (CMC).
  • MC methylcellulose
  • EC ethyl cellulose
  • HEC hydroxyethyl cellulose
  • HPC hydroxypropyl cellulose
  • EH EC ethyl hydroxyethyl cellulose
  • EHPC ethylhydroxypropyl cellulose
  • MHPC methylhydroxypropylcellulose
  • CMC carboxymethyl cellulose
  • Polysaccharides are present in the plaster composition at from 0.01 to 99.9 percent by weight, preferably 0.01 to 50 percent by weight, and most preferably 0.01 to 10 percent by weight, based on the dry composition.
  • the aging stabilizer is a compound or compounds that provide age stability to the composition.
  • Aging stabilizers include, but are not limited to, one or more amino acids, amines, carboxylic acids, thiols, amides; and polymers containing amino acid, amine, carboxylic acid, thiol, or amides functionality.
  • the amount of aging stabilizer in the dry composition is in the range of 0.0001 to 50 percent by weight, preferably from 0.0001 to 20 percent by weight, and most preferably from 0.0001 to 2 percent by weight.
  • the ratio of aging stabilizer to polysaccharide and binder, on a solids basis is in the range of 1 part aging stabilizer to 1 to 200 parts of polysaccharide, and 1 to 1000 parts of organic polymer binder.
  • a preferred class of aging stabilizers are amino acids.
  • Amino acids useful in the present invention include, but are not limited to alanine, arginine, asparagine, aspartic acid, cysteine, cystine, 3,5-dibromotyrosine, diiodotyrosine, glutamic acid, glutamine, glycine, histidine, hydroxylysine, hydroxyproline, isoleucine, leucine, lysine, methionine, phenylalanine, proline, serine, threonine, thyroxine, tryptophane, tyrosine, valine.
  • a particularly preferred amino acid is glycine.
  • the amino acids in the composition preferably have good water solubility. Solubility of the amino acids may be increased by full or partial neutralization to form amino acid salts.
  • the amino-acid salts are in the form of sodium, potassium, ammonium, and calcium salts.
  • a functional polymer incorporating one or more amino acid, amine, amide, carboxylic acid, and/or thiol functional groups may also serve as the aging stabilizer.
  • the functional groups may be incorporated by many methods, including but not limited to homopolymerization of a functional monomer, copolymerization of one or more functional monomers with one or more non-functional monomer, grafting of a functionality onto the polymer backbone, post-polymerization reactions, or other means known in the art.
  • Examples of functional monomer includes, but is not limited to, acrylic acid, 2-acrylamido-2-methyl propane sulfonic acid, sodium methallyl sufonate, sodium vinyl sulfonate, sulfonated styrene, allyloxybenzene sulfonic acid, methacrylic acid, ethacrylic acid, alpha-chloro-acrylic acid, alpha-cyano acrylic acid, alpha-chloro-acrylic acid, alpha-cyano acrylic acid, beta methyl-acrylic acid (crotonic acid), alpha-phenyl acrylic acid, beta-acryloxy propionic acid, sorbic acid, alpha-chloro sorbic acid, angelic acid, cinnamic acid, p-chloro cinnamic acid, beta-styryl acrylic acid (1-carboxy-4-phenyl butadiene-1,3), itaconic acid, maleic acid, citraconic acid, mesaconic acid, glutaconic
  • Aromatic amine containing monomers such as vinyl pyridine may also be used. Furthermore, monomers such as vinyl formamide, vinylacetamide etc which generate amine moieties on hydrolysis may also be used. N,N-dimethylaminoethyl methacrylate, N,N-dimethylaminopropyl methacrylamide. N,N dialkylaminoalkyl(meth)acrylate, N,N dialkylminoalkylacrylate, dialkylaminoalkyl(meth)acrylamide and N,N dialkylminoalkylacrylamide, where the alkyl groups are independently C 1-18 . Aromatic amine containing monomers such as vinyl pyridine may also be used.
  • hydrophilic acid-neutralizable monomer is N,N-dimethylaminoethyl methacrylate, and N,N-dimethylaminopropyl methacrylamide, carboxylic, dicarboxylic, sulfonic, and phosphonic acids, or mixtures thereof.
  • Examples of said monomers useful in the present invention include, but are not limited to acrylic acid, methacrylic acid, maleic anhydride, itaconic acid, crotonic acid, styrene sulfonic acid, 2-acrylamido-2-methylpropane sulfonic acid, vinyl sulfonic acid, ethacrylic acid, alpha-chloro-acrylic acid, alpha-cyano acrylic acid, beta methyl-acrylic acid (crotonic acid), alpha-phenyl acrylic acid, sorbic acid, alpha-chloro sorbic acid, angelic acid, cinnamic acid, p-chloro cinnamic acid, beta-styryl acrylic acid (1-carboxy-4-phenyl butadiene-1,3), itaconic acid, maleic acid, citraconic acid, mesaconic acid, glutaconic acid, aconitic acid, fumaric acid, tricarboxy ethylene, 2-acryloxypropionic acid
  • the binder of the invention is an organic polymer binder.
  • the polymer may be any known synthetic polymer, copolymer, or mixture thereof.
  • the polymer should be film-forming and water-soluble or water-dispersible.
  • the polymer may be synthesized by solution, emulsion, inverse emulsion, suspension or other polymerization method.
  • the polymer may be random, block, star, or other known polymer architecture.
  • Polymers useful in a building composition will typically have a Tg in the range of from ⁇ 60° C. to +40° C. In a dry composition, the polymer must be easily redispersible in water.
  • the polymer binder is present in the composition at a level of from 0.01 to 99.9 percent, preferably from 0.01 to 90 percent, and most preferably from 0.01 to 50 percent, based on the dry weight of polymer to dry weight of the composition.
  • a preferred class of polymers are emulsion polymers formed from ethylenically unsaturated monomers.
  • Useful monomer include, but not limited to, (meth)acrylates, maleates, (meth)acrylamides, vinyl esters, itaconates, styrenics, unsaturated hydrocarbons and acrylonitrile, nitrogen functional monomers, vinyl esters, ethylene, and alcohol functional monomers.
  • Particularly useful polymers include vinyl acetate homopolymers; ethylene/vinyl ester copolymers such as vinyl acetate/ethylene copolymers (EVA), EVAs with other comonomers, ethylene/vinyl versatate copolymers; vinyl ester/(meth)acrylate copolymers; styrene/acrylic copolymers; styrene butadiene copolymers.
  • the polymer is synthesized using polyvinyl alcohol as the stabilizer.
  • the polymer binder is free of carboxylic- and (meth)acrylamide- functional monomer units.
  • the polymeric binder may also contain some cationic functionality, and may be produced by the method described in U.S. patent applications Ser. No. 09/744,089 (WO 200005283), and Ser. No. 09/744,082 (WO 200005275), incorporated herein by reference.
  • one or more adjuvants may also be present in the composition at from 0 to 99.9 percent, preferably 0 to 99 percent and most preferably from 5 to 98 percent by weight, based on the composition solids.
  • These adjuvants may be one or more compounds selected from inorganic binders, accelerators, retarders, fillers, wetting agents, defoamers, superplasticizers, coalescing agents, plasticizers, and other additives known in the art.
  • Typical fillers include, but are not limited to, calcium carbonate, sand, quartz, silica, kaolin, barium sulfate, titanium oxide, talc, and hydrated alumina.
  • Inorganic binder adjuvants include, but are not limited to, gypsum, and lime. When inorganic binders are used in the composition, they are generally present at from 10 to 99.9 percent by weight, preferably from 15 to 99 percent by weight, and most preferably from 20 to 98 percent by weight. A mixture of both organic polymer binder and inorganic binder in the composition may be useful to obtain the best level of product performance and cost.
  • the composition of the invention includes one or more superplasticizers.
  • superplasticizers also known as cement superplasticizers include, but are not limited to, casein and other natural substances, melamine-formaldehyde condensates, sulfonated napthalin-formaldehyde condensates, modified lignosulfonates, polycarboxylates, polyacrylates, polystyrene sulfonates, and sulfonic esters.
  • the superplasticizer is present in the composition at a ratio of 0.01 to 2 parts of superplasticizer to 1 part polysaccharide, on a weight to weight basis.
  • the individual components may be combined in any number of ways, and in any combination, to form the final composition of the present invention. All components may be formed into the dry state, and be admixed together. Two or more ingredients may be combined in a wet state, and dried together.
  • the polymer binder may be functionalized with the aging stabilizer either through the copolymerization of a functional monomer, or a post-polymerization reaction.
  • the polysaccharide and/or aging stabilizer may be combined with a latex polymer, and the mixture dried by means known in the art, such as by spray-drying, freeze-drying, or drum drying.
  • the polysaccharide and/or aging stabilizer may also be associated with a polymer dispersant, such as polyvinyl alcohol, which may be used as a stabilizer in an emulsion polymerization of a polymer additive.
  • the polysaccharide and/or aging stabilizer may be combined with an aqueous polymer solution or emulsion in a spray-drying tower, and sprayed and dried together.
  • the polysaccharide and/or aging stabilizer may be dried in separate operations, then the dry components blended together.
  • Another process involves combining the polysaccharide and aging stabilizer. This combination can either be added in an aqueous dispersion with other ingredients, or the combination may be dried, then admixed with other dry ingredients.
  • compositions of the present invention will have a pH of from 4 to 10 when blended with water into a 50 percent by weight paste. At higher pH, the problems associated with polysaccharide degradation are mitigated by the highly alkaline environment.
  • compositions of the invention may be used in several end-use applications.
  • a particularly preferred application would be as a building composition.
  • One building application of the composition is as a plaster.
  • the plaster typically contains gypsum or lime as the binder, and will often also contain some organic polymer binder for improved properties such as adhesion.
  • a dry gypsum plaster or mortar composition is one that is ready to use with the addition of only water.
  • Some uses for the plaster include, but are not limited to coatings, surfacing plasters, projection plasters, plasters for smooth supports, plasters for floor finishing, plasters for facing of imitation brickwork, plaster for both exterior and interior coatings.
  • the plaster may be in the form of a redispersible powder, a fluid paste, hardened paste, or finished products.
  • the building composition is also useful for forming gypsum boards.
  • Gypsum rich products may contain up to 99.9 percent by weight of gypsum.
  • Filled-gypsum products contain about 30 percent gypsum and a large amount of filler.
  • the dry building composition may also be a gypsum-free, cement-free plaster composition.
  • a gypsum-free building composition typically exists as an aqueous-based dispersion or paste containing a polymer binder, filler, polysaccharide, and the aging stabilizer.
  • the gypsum-free composition is useful for formulating ceramic tile adhesive (CTA), repair mortar, and other known gypsum-free products.
  • the polymer binder is present at from 2 to 50 percent by weight, and preferably from 5 to 15 percent by weight, based on dry polymer to dry composition.
  • a one-pack gypsum-free product will typically contain from 7 to 15 percent by weight of polymer on a solids to solids basis.
  • the gypsum-free, cement-free composition may be combined with a cement just prior to final use, as part of a two-part system.
  • composition of the invention may also be a medicinal or pharmaceutical plaster, often used for applications involving the sustained release of active ingredients.
  • a dry gypsum formulation was prepared by blending 97.5 weight percent of alpha plaster gypsum, 0.5 percent by weight of cellulose ether (10-20 Pas), and 2 percent by weight of a redispersible polymer powder.
  • the polymer powder is an ethylene-vinyl acetate copolymer.
  • a dry gypsum formulation was prepared as in Example 1, using as the polymer powder an ethylene-vinyl acetate powder to which 1.6 percent by weight of glycine has been added prior to spray drying.
  • a dry gypsum formulation was prepared as in Example 2, using as the polymer powder an ethylene-vinyl acetate powder to which 0.5 percent by weight of glycine has been added.
  • a dry gypsum formulation was prepared as in Example 1, using as the polymer powder a vinyl acetate/VeoVa powder.
  • a dry gypsum formulation was prepared as in Example 2, using as the polymer powder a vinyl acetate/VeoVa powder to which 1.6 percent by weight of glycine has been added.
  • a dry gypsum formulation was prepared as in Example 1, using as the polymer powder a acrylic polymer powder.
  • a dry gypsum formulation was prepared as in Example 2, using as the polymer powder an acrylic powder to which 1.6 percent by weight of glycine has been added.
  • a gypsum plaster is formulated by blending 57.5 weight percent gypsum (alpha plaster), 40 weight percent calcium carbonate, 0.5 weight percent cellulose ether (10-20 Pas), and 2 weight percent of a redispersible powder of an ethylene-vinyl acetate copolymer containing 1.6 percent by weight glycine.
  • a two component ceramic tile adhesive is prepared by forming as component 1:
  • Component 1 and component 2 are then mixed in a ratio of about 80:20 to 70:30, directly before use.
  • a pasty ceramic tile adhesive is formulated by admixing

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
US10/346,267 2003-01-16 2003-01-16 Age-stable composition having a polysaccharide Abandoned US20040143038A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US10/346,267 US20040143038A1 (en) 2003-01-16 2003-01-16 Age-stable composition having a polysaccharide
PCT/US2004/000461 WO2004065320A2 (fr) 2003-01-16 2004-01-08 Age-stable composition having a polysaccharide
EP04700899A EP1583725A2 (fr) 2003-01-16 2004-01-08 Age-stable composition having a polysaccharide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10/346,267 US20040143038A1 (en) 2003-01-16 2003-01-16 Age-stable composition having a polysaccharide

Publications (1)

Publication Number Publication Date
US20040143038A1 true US20040143038A1 (en) 2004-07-22

Family

ID=32712104

Family Applications (1)

Application Number Title Priority Date Filing Date
US10/346,267 Abandoned US20040143038A1 (en) 2003-01-16 2003-01-16 Age-stable composition having a polysaccharide

Country Status (3)

Country Link
US (1) US20040143038A1 (fr)
EP (1) EP1583725A2 (fr)
WO (1) WO2004065320A2 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070004828A1 (en) * 2005-07-01 2007-01-04 Akzo Nobel Coatings International B.V. Adhesive system and method
US20070004829A1 (en) * 2005-07-01 2007-01-04 Akzo Nobel Coatings International B.V. Adhesive composition and method
US20080233390A1 (en) * 2005-08-16 2008-09-25 Alexander Gothlich Polymer Composition For Corrosion Protection
US20090317651A1 (en) * 2006-06-23 2009-12-24 Akzo Nobel Coatings International B.V. Adhesive system and method of producing a wood based product
US8048257B2 (en) 2006-06-23 2011-11-01 Akzo Nobel Coating International B.V. Adhesive system and method of producing a wood based product
CN105367030A (zh) * 2015-11-06 2016-03-02 江苏尼高科技有限公司 脱硫石膏基轻质喷涂石膏砂浆
CN114195431A (zh) * 2021-12-16 2022-03-18 平潭智汇畅城科技有限公司 一种高分子砂浆

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3652309A (en) * 1969-04-01 1972-03-28 United States Gypsum Co Retarded gypsum plaster for use in long set aggregated mortar applications
US5534059A (en) * 1995-03-20 1996-07-09 United States Gypsum Co. Machinable plaster
US5932001A (en) * 1996-05-15 1999-08-03 Roquette Freres Plaster composition containing an amylaceous compound
US5959029A (en) * 1995-01-26 1999-09-28 National Starch And Chemical Investment Holding Corporation Composition containing a styrene/methacrylate polymer
US6080806A (en) * 1996-01-10 2000-06-27 Rhodia Chimie Water-redispersible powders of film-forming polymers prepared from ethylenically unsaturated monomers
US6367550B1 (en) * 2000-10-25 2002-04-09 Halliburton Energy Service, Inc. Foamed well cement slurries, additives and methods
US6402832B1 (en) * 2000-05-15 2002-06-11 Fleetwood Enterprise, Inc. A Delaware Corporation Wallboard joint compound
US6409825B1 (en) * 2000-11-22 2002-06-25 United States Gypsum Company Wet gypsum accelerator and methods, composition, and product relating thereto
US6565645B1 (en) * 1998-04-17 2003-05-20 Henkel Kommanditgesellschaft Auf Aktien Water-resistant hydraulically setting compositions

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3652309A (en) * 1969-04-01 1972-03-28 United States Gypsum Co Retarded gypsum plaster for use in long set aggregated mortar applications
US5959029A (en) * 1995-01-26 1999-09-28 National Starch And Chemical Investment Holding Corporation Composition containing a styrene/methacrylate polymer
US5534059A (en) * 1995-03-20 1996-07-09 United States Gypsum Co. Machinable plaster
US6080806A (en) * 1996-01-10 2000-06-27 Rhodia Chimie Water-redispersible powders of film-forming polymers prepared from ethylenically unsaturated monomers
US5932001A (en) * 1996-05-15 1999-08-03 Roquette Freres Plaster composition containing an amylaceous compound
US6565645B1 (en) * 1998-04-17 2003-05-20 Henkel Kommanditgesellschaft Auf Aktien Water-resistant hydraulically setting compositions
US6402832B1 (en) * 2000-05-15 2002-06-11 Fleetwood Enterprise, Inc. A Delaware Corporation Wallboard joint compound
US6367550B1 (en) * 2000-10-25 2002-04-09 Halliburton Energy Service, Inc. Foamed well cement slurries, additives and methods
US6409825B1 (en) * 2000-11-22 2002-06-25 United States Gypsum Company Wet gypsum accelerator and methods, composition, and product relating thereto

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070004828A1 (en) * 2005-07-01 2007-01-04 Akzo Nobel Coatings International B.V. Adhesive system and method
US20070004829A1 (en) * 2005-07-01 2007-01-04 Akzo Nobel Coatings International B.V. Adhesive composition and method
US7960452B2 (en) * 2005-07-01 2011-06-14 Akzo Nobel Coatings International B.V. Adhesive composition and method
US8147979B2 (en) 2005-07-01 2012-04-03 Akzo Nobel Coatings International B.V. Adhesive system and method
US20080233390A1 (en) * 2005-08-16 2008-09-25 Alexander Gothlich Polymer Composition For Corrosion Protection
US8420174B2 (en) * 2005-08-16 2013-04-16 Basf Se Polymer composition for corrosion protection
US20090317651A1 (en) * 2006-06-23 2009-12-24 Akzo Nobel Coatings International B.V. Adhesive system and method of producing a wood based product
US8048257B2 (en) 2006-06-23 2011-11-01 Akzo Nobel Coating International B.V. Adhesive system and method of producing a wood based product
CN105367030A (zh) * 2015-11-06 2016-03-02 江苏尼高科技有限公司 脱硫石膏基轻质喷涂石膏砂浆
CN114195431A (zh) * 2021-12-16 2022-03-18 平潭智汇畅城科技有限公司 一种高分子砂浆

Also Published As

Publication number Publication date
WO2004065320A3 (fr) 2004-12-29
WO2004065320A2 (fr) 2004-08-05
EP1583725A2 (fr) 2005-10-12

Similar Documents

Publication Publication Date Title
JP4950877B2 (ja) ポリマー組成物および水性建築材料系および水ベース塗料系およびコーティング系への添加剤としてのその使用
JP5553748B2 (ja) 硫酸カルシウム系乾式建設材料混合物
JP5473178B2 (ja) 水溶性または水膨潤性スルホ基含有会合性増粘コポリマー、その製法
US6187887B1 (en) Water-soluble or water-swellable copolymers containing sulfonic groups and methods of preparation
US7605196B2 (en) Water-soluble copolymers containing sulfo groups, method for the production and use thereof
US7988783B2 (en) Additive for hydraulically setting systems, the hydraulically setting mixtures and the use there of
TWI253953B (en) Dispersants
JPH11503790A (ja) 再分散性のポリマー粉末および該粉末から得られる水性ポリマー分散液
CN100586998C (zh) 用保护胶体稳定化的分散粉末
JP2007534605A (ja) 水分保持剤を用いたタイル用セメントモルタル
JPH05201756A (ja) 建材用の水−含有混合物の加工性を改良するための添加剤の組み合わせ
MXPA06012319A (es) Morteros basados en yeso que usan agentes de retencion de agua preparados de borras de algodon crudo.
US8828137B2 (en) Additive composition for mortars, cements and joint compounds and cementitious compositions made therefrom
US6429251B2 (en) Polyvinyl alcohol-stabilized 1,3-diene/ (meth)acrylate copolymers
BRPI1103860A2 (pt) cimento, e , mÉtodo de vedaÇço, ligaÇço ou revestimento de um substrato
PT1984453E (pt) PROCESSO PARA A PRODUÆO DE CORPOS MOLDADOS A PARTIR DE UMA MISTURA DE MATERIAIS NATURAIS GRANULARES E DE UM AGLUTINANTE TERMOPLáSTICO
BRPI1103218A2 (pt) pó de polìmero redispersável em água, métodos para produzir um pó de polìmero redispersável em água, e para preparar uma composição de cimento, e , formulação de mistura a seco
BR112014013241B1 (pt) composição de mistura seca contendo cimento
US8882907B2 (en) Additive composition for mortars, cements and joint compounds and cementitious compositions made therefrom
JP2010527397A (ja) コポリマー混合物
JP3162725B2 (ja) エチレン性不飽和を含有する単量体から製造された皮膜形成性重合体の水に再分散できる粉末
US20040143038A1 (en) Age-stable composition having a polysaccharide
CN1487016A (zh) 可再分散的分散体粉末组合物、其用途及其制备方法
JP4654455B2 (ja) 水溶性のスルホ基含有ビポリマーおよびターポリマー、その製造方法ならびに水性建築材料系、水性塗料系および水性被覆系のための安定剤としてのその使用
JPH0459324B2 (fr)

Legal Events

Date Code Title Description
AS Assignment

Owner name: NATIONAL STARCH AND CHEMICAL INVESTMENT HOLDING CO

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ABERLE, THOMAS;REEL/FRAME:013689/0860

Effective date: 20030113

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION